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4-Fluoro-bicyclo[2.2.2]octan-1-amine is a unique chemical compound belonging to the class of amines, distinguished by the presence of a fluorine atom on its bicyclic octane structure. 4-Fluoro-bicyclo[2.2.2]octan-1-aMine is known for its potential applications in the pharmaceutical and agrochemical industries due to its distinctive structural features and reactivity. The fluorine atom in its structure may confer specific properties that are advantageous for various applications, making 4-Fluoro-bicyclo[2.2.2]octan-1-amine an intriguing and versatile chemical entity with broad utility across different fields.

78385-91-8

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78385-91-8 Usage

Uses

Used in Pharmaceutical Industry:
4-Fluoro-bicyclo[2.2.2]octan-1-amine is utilized as a building block in the synthesis of diverse organic compounds and pharmaceutical agents. Its unique structure and reactivity contribute to the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Fluoro-bicyclo[2.2.2]octan-1-amine serves as a key intermediate in the production of various agrochemicals, including pesticides and herbicides. Its incorporation into these compounds can enhance their performance and selectivity, leading to more effective and environmentally friendly products.
Used in Organic Synthesis:
4-Fluoro-bicyclo[2.2.2]octan-1-amine is employed as a versatile starting material in organic synthesis, allowing for the creation of a wide range of chemical entities. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules with potential applications in various industries.
Used in Fluorine Chemistry:
The presence of the fluorine atom in 4-Fluoro-bicyclo[2.2.2]octan-1-amine makes it an interesting compound in the field of fluorine chemistry. Fluorine is known for its unique properties, such as high electronegativity and small size, which can significantly influence the physical and chemical properties of molecules. 4-Fluoro-bicyclo[2.2.2]octan-1-aMine can be used to explore the effects of fluorination on various chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 78385-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,8 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 78385-91:
(7*7)+(6*8)+(5*3)+(4*8)+(3*5)+(2*9)+(1*1)=178
178 % 10 = 8
So 78385-91-8 is a valid CAS Registry Number.

78385-91-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluorobicyclo(2.2.2)octan-1-amine

1.2 Other means of identification

Product number -
Other names 4-fluorobicyclo[2.2.2]octan-1-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:78385-91-8 SDS

78385-91-8Downstream Products

78385-91-8Relevant academic research and scientific papers

BICYCLO DERIVATIVE

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Page/Page column 8, (2008/06/13)

A novel bicyclo derivative represented by the following general formula (1), or a pharmaceutically acceptable salt thereof, acts as an effective DPP-IV inhibitor: One example is (2S,4S)-1-[[N-(4-methylbicyclo[2.2.2]oct-1-yl)amino]acetyl]-4-fluoropyrrolidi

Synthesis of 4-Substituted Bicyclooct-1-yl Fluorides

Adcock, William,Abeywickrema, Anil N.

, p. 2951 - 2957 (2007/10/02)

The main details of the synthesis of a series of 4-substituted (X) bicyclooct-1-yl fluorides (1), which were required for substituent effect studies, are presented.The synthesis of most of these compounds 1, X = NO2, CN, CONH2, COCH3, CHO, OCH3, O

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